NDC 82709-001 Innoble Onechewtoothpaste

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82709-001
Proprietary Name:
Innoble Onechewtoothpaste
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Livmate
Labeler Code:
82709
Start Marketing Date: [9]
05-03-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
10 MM
Score:
1

Product Packages

NDC Code 82709-001-01

Package Description: 84 g in 1 POUCH

NDC Code 82709-001-03

Package Description: 1 BOTTLE, GLASS in 1 CARTON / 42 g in 1 BOTTLE, GLASS (82709-001-02)

Product Details

What is NDC 82709-001?

The NDC code 82709-001 is assigned by the FDA to the product Innoble Onechewtoothpaste which is product labeled by Livmate. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 82709-001-01 84 g in 1 pouch , 82709-001-03 1 bottle, glass in 1 carton / 42 g in 1 bottle, glass (82709-001-02). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Innoble Onechewtoothpaste?

Adults and children 6 years of age and older; Gently chew 1 tablet until it crushed. Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.

Which are Innoble Onechewtoothpaste UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Innoble Onechewtoothpaste Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".